Detrimental Effects of Diet-Induced Obesity on τ Pathology Are Independent of Insulin Resistance in τ Transgenic Mice

Author:

Leboucher Antoine12,Laurent Cyril12,Fernandez-Gomez Francisco-José12,Burnouf Sylvie12,Troquier Laetitia12,Eddarkaoui Sabiha12,Demeyer Dominique12,Caillierez Raphaëlle12,Zommer Nadège12,Vallez Emmanuelle134,Bantubungi Kadiombo134,Breton Christophe15,Pigny Pascal126,Buée-Scherrer Valérie12,Staels Bart134,Hamdane Malika12,Tailleux Anne134,Buée Luc126,Blum David126

Affiliation:

1. Université Lille-Nord de France, Université du Droit et de la Santé de Lille, Lille, France

2. INSERM U837, Jean-Pierre Aubert Research Centre, Institut de Médecine Prédictive et de Recherche Thérapeutique, Lille, France

3. INSERM U1011, Lille, France

4. Institut Pasteur de Lille, Lille, France

5. EA 4489, Environnement Perinatal et Croissance, Lille, France

6. Centre Hospitalier Régional Universitaire de Lille, Lille, France

Abstract

The τ pathology found in Alzheimer disease (AD) is crucial in cognitive decline. Midlife development of obesity, a major risk factor of insulin resistance and type 2 diabetes, increases the risk of dementia and AD later in life. The impact of obesity on AD risk has been suggested to be related to central insulin resistance, secondary to peripheral insulin resistance. The effects of diet-induced obesity (DIO) on τ pathology remain unknown. In this study, we evaluated effects of a high-fat diet, given at an early pathological stage, in the THY-Tau22 transgenic mouse model of progressive AD-like τ pathology. We found that early and progressive obesity potentiated spatial learning deficits as well as hippocampal τ pathology at a later stage. Surprisingly, THY-Tau22 mice did not exhibit peripheral insulin resistance. Further, pathological worsening occurred while hippocampal insulin signaling was upregulated. Together, our data demonstrate that DIO worsens τ phosphorylation and learning abilities in τ transgenic mice independently from peripheral/central insulin resistance.

Publisher

American Diabetes Association

Subject

Endocrinology, Diabetes and Metabolism,Internal Medicine

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